Canonical Allele Identifier: CA5967025

Gene: F2

Linked Data

• dbSNP Id: rs775856487
• ExAC: 11:46747489 G / A
• gnomAD v2: 11-46747489-G-A
• gnomAD v4: 11-46725939-G-A
• MyVariant Identifiers: chr11:g.46747489G>A (hg19) ; chr11:g.46725939G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725939G>A , CM000673.2:g.46725939G>A	GRCh38
NC_000011.9:g.46747489G>A , CM000673.1:g.46747489G>A	GRCh37
NC_000011.8:g.46704065G>A	NCBI36
NG_008953.1:g.11747G>A , LRG_551:g.11747G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.640G>A MANE Select	ENSP00000308541.5:p.Val214Ile
ENST00000311907.9:c.640G>A	ENSP00000308541.5:p.Val214Ile
ENST00000442468.1:c.610G>A	ENSP00000387413.1:p.Val204Ile
ENST00000490274.1:n.420G>A
ENST00000530231.5:c.640G>A	ENSP00000433907.1:p.Val214Ile
NM_000506.3:c.640G>A	NP_000497.1:p.Val214Ile
NM_000506.4:c.640G>A , LRG_551t1:c.640G>A	NP_000497.1:p.Val214Ile
NM_001311257.1:c.592G>A	NP_001298186.1:p.Val198Ile
XR_428840.2:n.684G>A
XR_428840.4:n.675G>A
NM_000506.5:c.640G>A MANE Select	NP_000497.1:p.Val214Ile
NM_001311257.2:c.592G>A	NP_001298186.1:p.Val198Ile